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Anmuth Medical International

FDA UDI

Class I (US FDA UDI)

by Anmuth Medical International Llc

Identity

Trade Name
Anmuth Medical International FDA UDI
Generic Name
Corneal marker, single-use FDA UDI
Device Name
Pitanguy Flap Demarcator small, 5.0 mm wide, 6-1/4" (15.9 cm) FDA UDI
Model / Reference
72-181-16 FDA UDI
Description
Pitanguy Flap Demarcator small, 5.0 mm wide, 6-1/4" (15.9 cm) FDA UDI

Identifiers

Catalog Number
72-181-16 FDA UDI
Primary DI / UDI-DI
08403207009340 FDA UDI
FDA Product Code
FZZ FDA UDI
GMDN Term
Corneal marker, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 6.25 Inch FDA UDI

Category: Corneal marker, single-use

Anmuth Medical International by Anmuth Medical International Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneal marker, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fda97b00-9782-4391-83d8-df83a837fe47 36 fields · synced May 31, 2026